Variant report

Variant	nsv1007685
Chromosome Location	chr4:79732468-79788768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79785292-79785904	K562	blood:	n/a	n/a
2	ARID3A	chr4:79783432-79784100	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:79785579-79785957	HepG2	liver:	n/a	n/a
4	ATF2	chr4:79766511-79767010	GM12878	blood:	n/a	n/a
5	BACH1	chr4:79742405-79742478	K562	blood:	n/a	n/a
6	BHLHE40	chr4:79785593-79785894	HepG2	liver:	n/a	n/a
7	BHLHE40	chr4:79785583-79785928	K562	blood:	n/a	n/a
8	BHLHE40	chr4:79785560-79785921	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:79785696-79785848	A549	lung:	n/a	n/a
10	CBX3	chr4:79783417-79783810	K562	blood:	n/a	n/a
11	CCNT2	chr4:79784481-79784683	K562	blood:	n/a	n/a
12	CEBPB	chr4:79767474-79767766	K562	blood:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
13	CEBPB	chr4:79767431-79767721	HepG2	liver:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
14	CEBPB	chr4:79766768-79767081	IMR90	lung:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
15	CEBPB	chr4:79785678-79785861	A549	lung:	n/a	chr4:79785779-79785790
16	CEBPB	chr4:79783488-79783776	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:79766793-79767104	HepG2	liver:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
18	CEBPB	chr4:79785618-79785928	H1-hESC	embryonic stem cell:	n/a	chr4:79785779-79785790
19	CEBPB	chr4:79767439-79767774	Hela-S3	cervix:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
20	CEBPB	chr4:79785585-79785946	Hela-S3	cervix:	n/a	chr4:79785779-79785790
21	CEBPB	chr4:79785712-79785848	HepG2	liver:	n/a	chr4:79785779-79785790
22	CEBPB	chr4:79766793-79767090	A549	lung:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
23	CEBPB	chr4:79763289-79763593	K562	blood:	n/a	chr4:79763466-79763479
24	CEBPB	chr4:79783441-79783834	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:79740967-79741220	K562	blood:	n/a	chr4:79741199-79741208 chr4:79741071-79741082 chr4:79741071-79741082
26	CEBPB	chr4:79766845-79767080	K562	blood:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
27	CEBPB	chr4:79783471-79783801	A549	lung:	n/a	n/a
28	CEBPB	chr4:79767468-79767708	A549	lung:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
29	CEBPB	chr4:79783366-79783842	A549	lung:	n/a	n/a
30	CEBPB	chr4:79785594-79785955	K562	blood:	n/a	chr4:79785779-79785790
31	CEBPB	chr4:79785600-79785965	IMR90	lung:	n/a	chr4:79785779-79785790
32	CEBPB	chr4:79766781-79767118	Hela-S3	cervix:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
33	CEBPB	chr4:79785547-79785905	K562	blood:	n/a	chr4:79785779-79785790
34	CEBPB	chr4:79785536-79785864	MCF-7	breast:	n/a	chr4:79785779-79785790
35	CEBPB	chr4:79785697-79785893	K562	blood:	n/a	chr4:79785779-79785790
36	CEBPB	chr4:79785598-79785956	HepG2	liver:	n/a	chr4:79785779-79785790
37	CEBPB	chr4:79783392-79783770	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:79783440-79783884	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:79785614-79785936	A549	lung:	n/a	chr4:79785779-79785790
40	CEBPB	chr4:79785627-79785929	A549	lung:	n/a	chr4:79785779-79785790
41	CEBPB	chr4:79785583-79785902	MCF-7	breast:	n/a	chr4:79785779-79785790
42	CEBPB	chr4:79767434-79767778	IMR90	lung:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
43	CEBPB	chr4:79785493-79785990	HCT-116	colon:	n/a	chr4:79785779-79785790
44	CEBPB	chr4:79757946-79758020	K562	blood:	n/a	n/a
45	CEBPB	chr4:79783485-79783817	K562	blood:	n/a	n/a
46	CEBPB	chr4:79741073-79741088	IMR90	lung:	n/a	n/a
47	CEBPD	chr4:79783512-79783760	HepG2	liver:	n/a	n/a
48	CREB1	chr4:79766603-79767098	GM12878	blood:	n/a	n/a
49	CREB1	chr4:79766427-79767200	GM12878	blood:	n/a	n/a
50	CTCF	chr4:79785660-79785810	Hela-S3	cervix:	n/a	chr4:79785753-79785771 chr4:79785755-79785768 chr4:79785748-79785769 chr4:79785754-79785770

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79732488-79732538	H1-hESC	embryonic stem cell:	embryo
2	chr4:79732488-79732538	BE2_C	brain:	n/a
3	chr4:79732488-79732538	GM12892	blood:	n/a
4	chr4:79732488-79732538	HEEpiC	esophagus:	n/a
5	chr4:79732488-79732538	GM12891	blood:	n/a
6	chr4:79732488-79732538	SKMC	muscle:	n/a
7	chr4:79732488-79732538	MCF10A-Er-Src	breast:	n/a
8	chr4:79732488-79732538	ovcar-3	ovarian:	n/a
9	chr4:79732488-79732538	AG04449	skin:	fetal
10	chr4:79732488-79732538	A549	lung:	n/a
11	chr4:79732488-79732538	HepG2	liver:	n/a
12	chr4:79732488-79732538	GM12878	blood:	n/a
13	chr4:79732488-79732538	HL-60	blood:	n/a
14	chr4:79732488-79732538	AG04450	lung:	fetal
15	chr4:79732488-79732538	NHDF-neo	bronchial:	n/a
16	chr4:79732488-79732538	GM06990	blood:	n/a
17	chr4:79732488-79732538	NHBE	bronchial:	n/a
18	chr4:79732488-79732538	NT2-D1	testis:	n/a
19	chr4:79732488-79732538	HEK293	kidney:	embryo
20	chr4:79732488-79732538	PANC-1	pancreas:	n/a
21	chr4:79732488-79732538	PrEC	prostate:	n/a
22	chr4:79732488-79732538	HNPCEpiC	eye:	n/a
23	chr4:79732488-79732538	Hepatocyte	liver:	n/a
24	chr4:79732488-79732538	Hela-S3	cervix:	n/a
25	chr4:79732488-79732538	HAEpiC	amniotic membrane:	n/a
26	chr4:79732488-79732538	SK-N-SH	brain:	n/a
27	chr4:79732488-79732538	MCF-7	breast:	n/a
28	chr4:79732488-79732538	AG09309	skin:	n/a
29	chr4:79732488-79732538	HCM	heart:	n/a
30	chr4:79732488-79732538	GM19239	blood:	n/a
31	chr4:79732488-79732538	HRCEpiC	kidney:	n/a
32	chr4:79732488-79732538	RPTEC	kidney:	n/a
33	chr4:79732488-79732538	U87	brain:	n/a
34	chr4:79732488-79732538	HRE	kidney:	n/a
35	chr4:79732488-79732538	NB4	blood:	n/a
36	chr4:79732488-79732538	SAEC	small airway:	n/a
37	chr4:79732488-79732538	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:79732488-79732538	HCPEpiC	choroid plexus:	n/a
39	chr4:79732488-79732538	PFSK-1	brain:	n/a
40	chr4:79732488-79732538	ECC-1	luminal epithelium:	n/a
41	chr4:79732488-79732538	HRPEpiC	eye:	n/a
42	chr4:79732488-79732538	T-47D	breast:	n/a
43	chr4:79732488-79732538	SK-N-SH_RA	brain:	n/a
44	chr4:79732488-79732538	Caco-2	colon:	n/a
45	chr4:79732488-79732538	HCT-116	colon:	n/a
46	chr4:79732488-79732538	Jurkat	blood:	n/a
47	chr4:79732488-79732538	ProgFib	skin:	n/a
48	chr4:79732488-79732538	LNCaP	prostate:	n/a
49	chr4:79732488-79732538	SK-N-MC	brain:	n/a
50	chr4:79732488-79732538	IMR90	lung:	fetal

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:79697257..79699576-chr4:79770892..79773352,2	MCF-7	breast:
2	chr4:79674995..79676989-chr4:79751851..79754832,2	K562	blood:
3	chr4:79747042..79749439-chr4:79778018..79780903,2	K562	blood:
4	chr4:79760812..79762742-chr4:79764884..79766656,2	K562	blood:
5	chr4:79778433..79779969-chr4:79781094..79783460,2	MCF-7	breast:
6	chr4:79700005..79702087-chr4:79782609..79785586,2	MCF-7	breast:
7	chr4:79696750..79699065-chr4:79783549..79785777,2	MCF-7	breast:
8	chr4:79762332..79763887-chr4:79767751..79769373,2	K562	blood:
9	chr4:79571062..79573548-chr4:79735105..79737173,2	K562	blood:
10	chr4:79761242..79763220-chr4:79764884..79767301,3	K562	blood:
11	chr4:79700579..79703463-chr4:79781034..79782674,2	MCF-7	breast:
12	chr4:79697991..79698551-chr4:79785291..79786155,2	MCF-7	breast:
13	chr4:79731165..79732753-chr4:79743062..79744642,2	K562	blood:
14	chr4:79738518..79741060-chr4:79744387..79746561,2	MCF-7	breast:
15	chr4:79738518..79741060-chr4:79744387..79746561,2	MCF-7	breast:
16	chr4:79781020..79783476-chr4:79785688..79788652,2	K562	blood:
17	chr4:79769174..79772080-chr4:79784280..79787147,3	K562	blood:
18	chr4:79760812..79762742-chr4:79764884..79766656,2	K562	blood:
19	chr4:79743529..79746797-chr4:79749528..79753927,4	K562	blood:
20	chr4:79743529..79746797-chr4:79749528..79753927,4	K562	blood:
21	chr4:79720788..79722594-chr4:79731131..79733817,2	MCF-7	breast:
22	chr4:79546113..79548024-chr4:79757297..79759344,2	K562	blood:
23	chr4:79533300..79533874-chr4:79785234..79786042,4	MCF-7	breast:
24	chr4:79774563..79776854-chr4:79782145..79784064,2	K562	blood:
25	chr4:79769347..79772550-chr4:79776506..79778988,3	K562	blood:
26	chr4:79770645..79772901-chr4:79776506..79779680,4	K562	blood:
27	chr4:79781020..79783476-chr4:79785688..79788652,2	K562	blood:
28	chr4:79774563..79776854-chr4:79782145..79784064,2	K562	blood:
29	chr4:79530799..79532363-chr4:79783489..79785979,2	K562	blood:
30	chr4:79534139..79535020-chr4:79785264..79785948,2	MCF-7	breast:
31	chr4:79743779..79746797-chr4:79749010..79752930,4	K562	blood:
32	chr4:79473307..79475885-chr4:79776923..79779312,2	K562	blood:
33	chr4:79761242..79763220-chr4:79764884..79767301,3	K562	blood:
34	chr4:79513272..79514062-chr4:79785483..79786626,3	K562	blood:
35	chr4:79761796..79764662-chr4:79771041..79772636,2	K562	blood:
36	chr4:79719962..79721538-chr4:79737317..79739683,2	K562	blood:
37	chr4:79727891..79730446-chr4:79730868..79733426,2	K562	blood:
38	chr4:79770873..79773260-chr4:79781468..79783460,2	K562	blood:
39	chr4:79530033..79532299-chr4:79783489..79785388,2	K562	blood:
40	chr4:79731165..79732753-chr4:79743062..79744642,2	K562	blood:
41	chr4:79749269..79751904-chr4:79770998..79773929,2	K562	blood:
42	chr4:79779277..79780895-chr4:79788393..79790584,2	K562	blood:
43	chr4:79752709..79756121-chr4:79759039..79764017,4	K562	blood:
44	chr4:79743779..79746797-chr4:79749010..79752930,4	K562	blood:
45	chr4:78880483..78881154-chr4:79785075..79785771,2	K562	blood:
46	chr4:79696453..79698645-chr4:79751602..79753557,2	MCF-7	breast:
47	chr4:79778433..79779969-chr4:79781094..79783460,2	MCF-7	breast:
48	chr4:79762332..79763887-chr4:79767751..79769373,2	K562	blood:
49	chr4:79782620..79784445-chr4:79794037..79795842,2	K562	blood:
50	chr4:79785946..79789478-chr4:79791153..79794900,4	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANXA3-7	chr4:79786362-79786441	ucscGeneNc_uc003hlh_2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5096	chr4:79741918-79741938	MIMAT0020603

No data

Variant related genes	Relation type
MIR5096	TF binding region
BMP2K	TF binding region
MIR5096	CpG island
BMP2K	CpG island
ENSG00000260278	chromatin interactions
ENSG00000266270	chromatin interactions
ENSG00000138772	chromatin interactions
ENSG00000138756	chromatin interactions

Extended variants
information (count: 1974 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1974 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541336172	chr4:79732476-79732477	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375789245	chr4:79732492-79732493	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552899332	chr4:79732496-79732497	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6818376	chr4:79732560-79732561	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs190465907	chr4:79732571-79732572	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558324881	chr4:79732592-79732593	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115985011	chr4:79732610-79732611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182718246	chr4:79732629-79732630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150865422	chr4:79732642-79732643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549073050	chr4:79732669-79732670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34512115	chr4:79732682-79732683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565700945	chr4:79732721-79732722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534717586	chr4:79732783-79732784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139354341	chr4:79732807-79732808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370432624	chr4:79732855-79732856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187447580	chr4:79732879-79732880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs59030520	chr4:79732886-79732887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142889069	chr4:79732916-79732917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192145765	chr4:79732923-79732924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146085363	chr4:79732926-79732927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115873435	chr4:79732943-79732944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572200603	chr4:79732967-79732968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184038336	chr4:79732975-79732976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563968767	chr4:79733009-79733010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570527440	chr4:79733039-79733040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187768802	chr4:79733073-79733074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543759695	chr4:79733091-79733092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373970327	chr4:79733115-79733116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563497230	chr4:79733141-79733142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs143552989	chr4:79733158-79733159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542682564	chr4:79733159-79733160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192501221	chr4:79733189-79733190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528611639	chr4:79733208-79733209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61470194	chr4:79733211-79733212	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571554442	chr4:79733275-79733276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184132814	chr4:79733279-79733280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187005418	chr4:79733287-79733288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371804615	chr4:79733313-79733314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191799437	chr4:79733330-79733331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535625501	chr4:79733381-79733382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371869852	chr4:79733402-79733403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371607887	chr4:79733403-79733404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184434492	chr4:79733416-79733417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17003453	chr4:79733428-79733429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144154357	chr4:79733456-79733457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544057952	chr4:79733480-79733481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556600944	chr4:79733519-79733520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557252435	chr4:79733521-79733522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576433474	chr4:79733524-79733525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574021862	chr4:79733625-79733626	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79700200-79732800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:79714400-79748400	Weak transcription	Aorta	Aorta
3	chr4:79720800-79747800	Weak transcription	Osteobl	bone
4	chr4:79721200-79741400	Weak transcription	Thymus	Thymus
5	chr4:79721600-79747200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:79726600-79747800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:79727800-79748200	Weak transcription	NHEK	skin
8	chr4:79728400-79747200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:79728600-79733600	Weak transcription	Primary B cells from cord blood	blood
10	chr4:79728600-79737800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:79728600-79738200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:79728600-79747200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:79728800-79735000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr4:79729000-79747200	Weak transcription	Fetal Muscle Trunk	muscle
15	chr4:79729600-79734600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:79729800-79735000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr4:79730000-79733600	Enhancers	Primary B cells from peripheral blood	blood
18	chr4:79730400-79741400	Weak transcription	Primary T cells from cord blood	blood
19	chr4:79730800-79733800	Enhancers	Fetal Intestine Large	intestine
20	chr4:79731000-79733400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:79731200-79732600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:79731200-79732800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:79731400-79732600	Enhancers	Fetal Intestine Small	intestine
24	chr4:79731400-79735200	Weak transcription	NHDF-Ad	bronchial
25	chr4:79731400-79748600	Weak transcription	Pancreas	Pancrea
26	chr4:79731600-79747400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr4:79731600-79748000	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:79731800-79732600	Enhancers	K562	blood
29	chr4:79731800-79736000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:79731800-79738400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:79731800-79747200	Weak transcription	Left Ventricle	heart
32	chr4:79731800-79747400	Weak transcription	Liver	Liver
33	chr4:79732000-79733200	Weak transcription	Right Atrium	heart
34	chr4:79732000-79735600	Weak transcription	Psoas Muscle	Psoas
35	chr4:79732200-79732600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:79732200-79733200	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:79732200-79747000	Weak transcription	NHLF	lung
38	chr4:79732400-79734600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:79732400-79735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:79732400-79738400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:79732400-79739600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:79732400-79747200	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr4:79732400-79747800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr4:79732400-79759200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr4:79732600-79733000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:79732600-79733600	Weak transcription	K562	blood
47	chr4:79732600-79733800	Weak transcription	Fetal Intestine Small	intestine
48	chr4:79732800-79738400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr4:79733000-79745000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:79733200-79733400	Enhancers	Colon Smooth Muscle	Colon

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